Georgiou I - Search Results

1

Vitamin D receptor gene polymorphisms in multiple sclerosis patients in northwest Greece.

Sioka C, Papakonstantinou S, Markoula S, Gkartziou F, Georgiou A, Georgiou I, Pelidou SH, Kyritsis AP, Fotopoulos A. Sioka C, et al. Among authors: georgiou i, georgiou a. J Negat Results Biomed. 2011 May 5;10:3. doi: 10.1186/1477-5751-10-3. J Negat Results Biomed. 2011. PMID: 21545713 Free PMC article.

2

The Sp1 COLIA1 gene polymorphism, and not vitamin D receptor or estrogen receptor gene polymorphisms, determines bone mineral density in postmenopausal Greek women.

Efstathiadou Z, Kranas V, Ioannidis JP, Georgiou I, Tsatsoulis A. Efstathiadou Z, et al. Among authors: georgiou i. Osteoporos Int. 2001;12(4):326-31. doi: 10.1007/s001980170123. Osteoporos Int. 2001. PMID: 11420783

3

Combined estrogen receptor alpha and estrogen receptor beta genotypes influence the age of menarche.

Stavrou I, Zois C, Chatzikyriakidou A, Georgiou I, Tsatsoulis A. Stavrou I, et al. Among authors: georgiou i. Hum Reprod. 2006 Feb;21(2):554-7. doi: 10.1093/humrep/dei326. Epub 2005 Oct 6. Hum Reprod. 2006. PMID: 16210384

4

Association of estrogen receptor-alpha gene polymorphisms with stroke risk in patients with metabolic syndrome.

Lazaros L, Markoula S, Xita N, Giannopoulos S, Gogou P, Lagos G, Kyritsis AP, Georgiou I. Lazaros L, et al. Among authors: georgiou i. Acta Neurol Scand. 2008 Mar;117(3):186-90. doi: 10.1111/j.1600-0404.2007.00926.x. Epub 2007 Sep 14. Acta Neurol Scand. 2008. PMID: 17854418

5

Estrogen receptor alpha gene polymorphisms and stroke.

Markoula S, Lazaros L, Xita N, Giannopoulos S, Georgiou I, Kyritsis AP. Markoula S, et al. Among authors: georgiou i. Cerebrovasc Dis. 2008;26(3):338. doi: 10.1159/000151591. Epub 2008 Aug 23. Cerebrovasc Dis. 2008. PMID: 18724048 Free article. No abstract available.

6

Estrogen receptor alpha gene haplotypes and diplotypes in the risk of stroke.

Markoula S, Xita N, Lazaros L, Giannopoulos S, Kyritsis AP, Georgiou I. Markoula S, et al. Among authors: georgiou i. Stroke. 2008 Nov;39(11):e172-3; author reply e174. doi: 10.1161/STROKEAHA.108.523233. Epub 2008 Sep 25. Stroke. 2008. PMID: 18818400 No abstract available.

7

Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations.

Bouba I, Siomou E, Stefanidis CJ, Emmanouilidou A, Galidi A, Hatzi E, Markoula S, Mitsioni A, Siamopoulou A, Georgiou I. Bouba I, et al. Among authors: georgiou i. Pediatr Nephrol. 2009 Aug;24(8):1569-72. doi: 10.1007/s00467-009-1140-y. Epub 2009 Mar 3. Pediatr Nephrol. 2009. PMID: 19255789

8

Paraoxonase gene polymorphisms and stroke severity.

Lazaros L, Markoula S, Kyritsis A, Georgiou I. Lazaros L, et al. Among authors: georgiou i. Eur J Neurol. 2010 May;17(5):757-9. doi: 10.1111/j.1468-1331.2009.02860.x. Epub 2009 Nov 23. Eur J Neurol. 2010. PMID: 19930448

9

Developing a genomic-based point-of-care diagnostic system for rheumatoid arthritis and multiple sclerosis.

Kalatzis FG, Giannakeas N, Exarchos TP, Lorenzelli L, Adami A, Decarli M, Lupoli S, Macciardi F, Markoula S, Georgiou I, Fotiadis DI. Kalatzis FG, et al. Among authors: georgiou i. Annu Int Conf IEEE Eng Med Biol Soc. 2009;2009:827-30. doi: 10.1109/IEMBS.2009.5333743. Annu Int Conf IEEE Eng Med Biol Soc. 2009. PMID: 19964246

10

Endothelial nitric oxide synthase polymorphism (G894T) and nonarteritic anterior ischemic optic neuropathy.

Giannopoulos S, Markoula S, Asproudis I, Galidi A, Nikas A, Kyritsis AP, Georgiou I. Giannopoulos S, et al. Among authors: georgiou i. Vis Neurosci. 2010 Nov;27(5-6):183-5. doi: 10.1017/S0952523810000350. Epub 2010 Nov 15. Vis Neurosci. 2010. PMID: 21073768

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